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Bismuth Subsalicylate
Bismuth Subsalicylate - 62211-046-99 - (Bismuth Subsalicylate)
Drug Information of Bismuth Subsalicylate
| Product NDC: | 62211-046 |
| Proprietary Name: | Bismuth Subsalicylate |
| Non Proprietary Name: | Bismuth Subsalicylate |
| Active Ingredient(s): | 262 mg/1 & nbsp; Bismuth Subsalicylate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Bismuth Subsalicylate
| Product NDC: | 62211-046 |
| Labeler Name: | A&Z Pharmaceutical, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part335 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20030310 |
Package Information of Bismuth Subsalicylate
| Package NDC: | 62211-046-99 |
| Package Description: | 15000 TABLET, CHEWABLE in 1 CARTON (62211-046-99) |
NDC Information of Bismuth Subsalicylate
| NDC Code | 62211-046-99 |
| Proprietary Name | Bismuth Subsalicylate |
| Package Description | 15000 TABLET, CHEWABLE in 1 CARTON (62211-046-99) |
| Product NDC | 62211-046 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Bismuth Subsalicylate |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20030310 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | A&Z Pharmaceutical, Inc. |
| Substance Name | BISMUTH SUBSALICYLATE |
| Strength Number | 262 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
